[go: up one dir, main page]

NO179904C - Condensed heterocyclic compounds and their use - Google Patents

Condensed heterocyclic compounds and their use

Info

Publication number
NO179904C
NO179904C NO933133A NO933133A NO179904C NO 179904 C NO179904 C NO 179904C NO 933133 A NO933133 A NO 933133A NO 933133 A NO933133 A NO 933133A NO 179904 C NO179904 C NO 179904C
Authority
NO
Norway
Prior art keywords
group
optionally substituted
substituted
hydrogen atom
hydrocarbon group
Prior art date
Application number
NO933133A
Other languages
Norwegian (no)
Other versions
NO933133D0 (en
NO933133L (en
NO179904B (en
Inventor
Hideaki Natsugari
Hitoshi Ikeda
Takenori Ishimaru
Takayuki Doi
Original Assignee
Takeda Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Takeda Chemical Industries Ltd filed Critical Takeda Chemical Industries Ltd
Publication of NO933133D0 publication Critical patent/NO933133D0/en
Publication of NO933133L publication Critical patent/NO933133L/en
Publication of NO179904B publication Critical patent/NO179904B/en
Publication of NO179904C publication Critical patent/NO179904C/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20Oxygen atoms
    • C07D215/22Oxygen atoms attached in position 2 or 4
    • C07D215/227Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/18Halogen atoms or nitro radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D215/54Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
    • C07D217/24Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
    • C07D217/26Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/36Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/50Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to ring nitrogen atoms
    • C07D241/52Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/06Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
    • C07D311/08Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
    • C07D311/18Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted otherwise than in position 3 or 7
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/76Benzo[c]pyrans
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Warehouses Or Storage Devices (AREA)

Abstract

Novel compound represented by the formula: <CHEM> wherein ring A may be substituted; ring B represents an optionally substituted benzene ring; either X or Y represents -NR<1>- (R<1> represents a hydrogen atom, an optionally substituted hydrocarbon group, an optionally substituted hydroxyl group or an optionally substituted amino group), -O- or -S-, the other representing -CO-, -CS- or -C(R<2>)R<2a>- (R<2> and R<2a> independently represent a hydrogen atom or an optionally substituted hydrocarbon group), or either X or Y represents -N=, the other representing =CR<3>- (R<3> represents a hydrogen atom, a halogen atom, an optionally substituted hydrocarbon group , an optionally substituted amino group, a substituted hydroxyl group or a mercapto group substituted by an optionally substituted hydrocarbon group); <........> represents a single or double bond; when <........> is a single bond, Z represents -CR<4>- (R<4> represents a hydrogen atom, hydroxyl group or an optionally substituted hydrocarbon group) or a nitrogen atom, or (ii) when <........> is a double bond, Z represents a carbon atom; D represents a C1-3 alkylene group which may be substituted by an oxo group or a thioxo group, or D and Y, taken together, may form a 5- to 7-membered ring which may be substituted by an oxo group or a thioxo group; E represents -NR<5>- (R<5> represents a hydrogen atom or an optionally substituted hydrocarbon group), -O- or -S(O)n- (n is 0,1 or 2), or R<5> and Y, taken together, may form a 5- to 7- membered ring which may be substituted by an oxo group or a thioxo group; G represents a bond or a C1-3 alkylene group; Ar represents an optionally substituted aryl group or an optionally substituted heterocyclic group, provided that (1) when (i) -X-Y- represents - O-CO- or -CO-O-, (ii) D represents -CO- and (iii) E represents -NR<5>-, either (a) G represents a C1-3 alkylene group and Ar represents a substituted aryl group or a substituted heterocyclic group, or (b) G represents a bond and R<5> represents an optionally substituted hydrocarbon group, and (2) when -X-Y- represents -NH-CO-, D represents -CO-, or a salt thereof having an excellent activity of inhibiting ACAT, lowering chlesterol in blood and inhibiting tachykinin recepter, or a salt thereof, their production and use.
NO933133A 1992-09-04 1993-09-02 Condensed heterocyclic compounds and their use NO179904C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP23748192 1992-09-04
JP10332893 1993-04-28

Publications (4)

Publication Number Publication Date
NO933133D0 NO933133D0 (en) 1993-09-02
NO933133L NO933133L (en) 1994-03-07
NO179904B NO179904B (en) 1996-09-30
NO179904C true NO179904C (en) 1997-01-08

Family

ID=26443975

Family Applications (1)

Application Number Title Priority Date Filing Date
NO933133A NO179904C (en) 1992-09-04 1993-09-02 Condensed heterocyclic compounds and their use

Country Status (13)

Country Link
US (2) US5482967A (en)
EP (1) EP0585913B1 (en)
KR (1) KR940007003A (en)
CN (1) CN1090274A (en)
AT (1) ATE161530T1 (en)
AU (1) AU667739B2 (en)
CA (1) CA2105518C (en)
DE (1) DE69315920T2 (en)
FI (1) FI933857A7 (en)
HU (1) HUT67284A (en)
IL (1) IL106908A0 (en)
NO (1) NO179904C (en)
NZ (1) NZ248583A (en)

Families Citing this family (96)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69422450T2 (en) * 1993-06-29 2000-06-08 Takeda Chemical Industries, Ltd. Quinolines or quinazoline derivatives and their use in the manufacture of a medicament for the treatment of osteoporosis
EP0634402A1 (en) * 1993-07-14 1995-01-18 Takeda Chemical Industries, Ltd. Isochinolinone derivatives, their production and use
WO1995009159A1 (en) * 1993-09-28 1995-04-06 Otsuka Pharmaceutical Company, Limited Quinoxaline derivative as antidiabetic agent
TW263498B (en) * 1993-11-10 1995-11-21 Takeda Pharm Industry Co Ltd
ATE273959T1 (en) * 1994-05-27 2004-09-15 Glaxosmithkline Spa QUINOLINE DERIVATIVES AS TACHYKININ NK3 RECEPTOR ANTAGONISTS
FR2725900B1 (en) * 1994-10-21 1997-07-18 Sanofi Sa USE OF NK1 RECEPTOR ANTAGONISTS FOR THE PREPARATION OF DRUGS WITH CARDIOREGULATORY ACTION
NO309272B1 (en) * 1995-03-24 2001-01-08 Takeda Chemical Industries Ltd Cyclic compounds, preparations containing the compounds and intermediates for the preparation of the compounds
US5770590A (en) * 1995-03-24 1998-06-23 Takeda Chemical Industries, Ltd. Cyclic compounds, their prudiction and use
AR004735A1 (en) * 1995-11-24 1999-03-10 Smithkline Beecham Spa CHINOLEIN 4-AMIDO SUBSTITUTED, A PROCEDURE FOR ITS PREPARATION, A PHARMACEUTICAL COMPOSITION THAT CONTAINS THEM AND THE USE OF THE SAME FOR THE PREPARATION OF A MEDICINAL PRODUCT.
GB9524104D0 (en) * 1995-11-24 1996-01-24 Smithkline Beecham Spa Novel compounds
ID18046A (en) * 1996-08-20 1998-02-19 Takeda Chemical Industries Ltd COMPOUND, MIXED CYCLE, MANUFACTURE AND USE OF IT.
KR100343832B1 (en) 1996-08-27 2002-07-20 시오노기세이야쿠가부시키가이샤 Chromene-3-carboxylate derivatives
KR20000057548A (en) * 1996-12-13 2000-09-25 알프레드 엘. 미첼슨 Optically transmissive material and bond
WO1998038168A1 (en) * 1997-02-27 1998-09-03 Tanabe Seiyaku Co., Ltd. Isoquinolinone derivatives, process for preparing the same, and their use as phosphodiesterase inhibitors
DE19755480A1 (en) * 1997-12-13 1999-06-24 Gruenenthal Gmbh Substituted heterocyclic benzocycloalkenes and their use as analgesic substances
FR2772761B1 (en) 1997-12-23 2000-05-26 Lipha NOVEL N-PHENYLAMIDE AND N-PYRIDYLAMIDE DERIVATIVES, THEIR PREPARATION METHOD AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
WO1999052519A2 (en) 1998-04-14 1999-10-21 The General Hospital Corporation Methods for treating neuropsychiatric disorders
JP4907818B2 (en) 1999-11-03 2012-04-04 エーエムアール テクノロジー インコーポレイテッド Aryl and heteroaryl substituted tetrahydroisoquinolines and their use to prevent reuptake of norepinephrine, dopamine and serotonin
US7163949B1 (en) 1999-11-03 2007-01-16 Amr Technology, Inc. 4-phenyl substituted tetrahydroisoquinolines and use thereof
FR2801310B1 (en) * 1999-11-24 2004-04-16 Adir NOVEL DIHYDROFURO- [3,4-b] QUINOLEIN-1-ONES DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
CN100430401C (en) 2000-07-11 2008-11-05 Amr科技公司 Novel 4-phenyl substituted tetrahydroisoquinolines and therapeutic use thereof
IL153633A0 (en) * 2000-07-13 2003-07-06 Takeda Chemical Insustries Ltd Lipid-rich plaque inhibitors
DE60132606T2 (en) * 2000-09-20 2009-02-19 Merck & Co., Inc. ISOCHINOLINONE AS CALIUM CHANNEL INHIBITORS
WO2002047723A1 (en) * 2000-12-11 2002-06-20 Takeda Chemical Industries, Ltd. Medicinal compositions having improved water-solubility
PL364221A1 (en) 2001-02-02 2004-12-13 Takeda Chemical Industries, Ltd. Fused heterocyclic compounds
EP1392283A4 (en) * 2001-05-16 2004-10-20 Cytovia Inc COUMARINS AND SUBSTITUTED QUINOLINES USED AS CASPASE ACTIVATORS
US20040152727A1 (en) * 2001-05-18 2004-08-05 Hay Douglas William Pierre Novel use
IL162810A0 (en) * 2002-01-11 2005-11-20 Takeda Pharmaceutical coumarin derivatives, process for their productionand use thereof
EP1484320A1 (en) * 2002-02-13 2004-12-08 Takeda Chemical Industries, Ltd. Jnk inhibitor
FR2849653B1 (en) * 2003-01-08 2006-08-25 B F B Etudes Et Rech S Experim COUMARIN DERIVATIVES HAVING AFFINITY FOR ESTROGEN RECEPTORS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME
EP1667982B1 (en) * 2003-09-23 2013-07-31 Merck Sharp & Dohme Corp. Isoquinolinone potassium channel inhibitors
EP1667978B1 (en) * 2003-09-23 2013-09-04 Merck Sharp & Dohme Corp. Isoquinolinone potassium channel inhibitors
AU2004276238B2 (en) 2003-09-23 2010-10-28 Merck Sharp & Dohme Corp. Isoquinolinone potassium channel inhibitors
CA2539546C (en) * 2003-09-23 2010-07-13 Merck & Co., Inc. Isoquinoline potassium channel inhibitors
WO2005030727A1 (en) * 2003-09-23 2005-04-07 Merck & Co., Inc. Isoquinolinone potassium channel inhibitors
WO2005068427A1 (en) * 2004-01-14 2005-07-28 Takeda Pharmaceutical Company Limited Carboxamide derivative and use thereof
RU2006134614A (en) 2004-03-02 2008-04-10 Такеда Фармасьютикал Компани Лимитед (Jp) KUMARIN DERIVATIVE AND ITS APPLICATION
PE20060285A1 (en) 2004-03-30 2006-05-08 Aventis Pharma Inc PYRIDONES SUBSTITUTE AS POL (ADP-RIBOSA) -POLYMERASE (PARP) INHIBITORS
RU2388751C2 (en) 2004-07-15 2010-05-10 Амр Текнолоджи, Инк. Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof for inhibiting norepinephrine, dopamine and serotonin reuptake
US8604055B2 (en) * 2004-12-31 2013-12-10 Dr. Reddy's Laboratories Ltd. Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors
WO2006073973A2 (en) 2004-12-31 2006-07-13 Reddy Us Therapeutics, Inc. Novel benzylamine derivatives as cetp inhibitors
WO2006095922A1 (en) * 2005-03-10 2006-09-14 Kyoto Pharmaceutical Industries, Ltd. Tetrahydroisoquinoline compound and medicinal use thereof
ES2382814T3 (en) 2005-05-17 2012-06-13 Merck Sharp & Dohme Ltd. Cis-4 - [(4-chlorophenyl) sulfonyl] -4- (2,5-difluorophenyl) cyclohexanopropanoic acid for cancer treatment
AR057325A1 (en) 2005-05-25 2007-11-28 Progenics Pharm Inc SYNTHESIS OF (S) -N-METHYLNTREXONE, PHARMACEUTICAL COMPOSITIONS AND USES
EA019115B1 (en) 2005-07-15 2014-01-30 Олбани Молекьюлар Рисерч, Инк. Aryl-and heteroaryl-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin
CA2642130C (en) * 2005-12-28 2013-04-02 Reddy Us Therapeutics, Inc. Selective benzylamine derivatives and their utility as cholesterol ester-transfer protein inhibitors
GB0603041D0 (en) 2006-02-15 2006-03-29 Angeletti P Ist Richerche Bio Therapeutic compounds
US7939545B2 (en) * 2006-05-16 2011-05-10 Boehringer Ingelheim International Gmbh Inhibitors of human immunodeficiency virus replication
US20110218176A1 (en) 2006-11-01 2011-09-08 Barbara Brooke Jennings-Spring Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
EP2805945B1 (en) 2007-01-10 2019-04-03 MSD Italia S.r.l. Amide substituted indazoles as poly(ADP-ribose)polymerase (PARP) inhibitors
US8389553B2 (en) 2007-06-27 2013-03-05 Merck Sharp & Dohme Corp. 4-carboxybenzylamino derivatives as histone deacetylase inhibitors
JP5269086B2 (en) * 2007-11-15 2013-08-21 ギリアード サイエンシス インコーポレーテッド Human immunodeficiency virus replication inhibitor
EA201200631A1 (en) * 2007-11-16 2012-11-30 Джилид Сайенсиз, Инк. Inhibitors of Human Immunodeficiency Virus Replication
US9156812B2 (en) 2008-06-04 2015-10-13 Bristol-Myers Squibb Company Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine
AR071997A1 (en) 2008-06-04 2010-07-28 Bristol Myers Squibb Co CRYSTAL FORM OF 6 - ((4S) -2-METHYL-4- (2-NAFTIL) -1,2,3,4-TETRAHYDROISOQUINOLIN-7-IL) PIRIDAZIN-3-AMINA
US8691825B2 (en) 2009-04-01 2014-04-08 Merck Sharp & Dohme Corp. Inhibitors of AKT activity
WO2010132487A1 (en) 2009-05-12 2010-11-18 Bristol-Myers Squibb Company CRYSTALLINE FORMS OF (S)-7-([1,2,4]TRIAZOLO[1,5-a]PYRIDIN-6-YL)-4-(3,4-DICHLOROHPHENYL)-1,2,3,4-TETRAHYDROISOQUINOLINE AND USE THEREOF
KR20120034644A (en) 2009-05-12 2012-04-12 알바니 몰레큘라 리써치, 인크. Aryl, heteroaryl, and heterocycle substituted tetrahydroisoquinolines and use thereof
CA2760837C (en) 2009-05-12 2018-04-03 Albany Molecular Research, Inc. 7-([1,2,4]triazolo[1,5-.alpha.]pyridin-6-yl)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydroisoquinoline and use thereof
BR112012008849A2 (en) 2009-10-14 2015-09-22 Schering Corp compound, pharmaceutical composition, and use of a compound
KR101883629B1 (en) 2010-01-20 2018-07-30 가부시키가이샤 한도오따이 에네루기 켄큐쇼 Semiconductor device
US8518907B2 (en) 2010-08-02 2013-08-27 Merck Sharp & Dohme Corp. RNA interference mediated inhibition of catenin (cadherin-associated protein), beta 1 (CTNNB1) gene expression using short interfering nucleic acid (siNA)
EP3587574B1 (en) 2010-08-17 2022-03-16 Sirna Therapeutics, Inc. Rna interference mediated inhibition of hepatitis b virus (hbv) gene expression using short interfering nucleic acid (sina)
EP2608669B1 (en) 2010-08-23 2016-06-22 Merck Sharp & Dohme Corp. NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
WO2012030685A2 (en) 2010-09-01 2012-03-08 Schering Corporation Indazole derivatives useful as erk inhibitors
US9242981B2 (en) 2010-09-16 2016-01-26 Merck Sharp & Dohme Corp. Fused pyrazole derivatives as novel ERK inhibitors
ES2663009T3 (en) 2010-10-29 2018-04-10 Sirna Therapeutics, Inc. Inhibition of RNA-mediated gene expression using short interference nucleic acids (ANic)
US9351965B2 (en) 2010-12-21 2016-05-31 Merck Sharp & Dohme Corp. Indazole derivatives useful as ERK inhibitors
US20120184548A1 (en) * 2011-01-19 2012-07-19 Romyr Dominique Carboxylic acid aryl amides
ES2602794T3 (en) 2011-03-31 2017-02-22 Pfizer Inc Novel bicyclic pyridinones
EP2699567A1 (en) 2011-04-21 2014-02-26 Merck Sharp & Dohme Corp. Insulin-like growth factor-1 receptor inhibitors
MX2014001849A (en) 2011-08-18 2014-10-24 Reddys Lab Ltd Dr Substituted heterocyclic amine compounds as cholestryl ester-transfer protein (cetp) inhibitors.
EP2760864B1 (en) 2011-09-27 2018-01-24 Dr. Reddy's Laboratories Ltd. 5-BENZYLAMINOMETHYL-6-AMINOPYRAZOLO[3,4-b]PYRIDINE DERIVATIVES AS CHOLESTERYL ESTER-TRANSFER PROTEIN (CETP) INHIBITORS USEFUL FOR THE TREATMENT OF ATHEROSCLEROSIS
WO2013063214A1 (en) 2011-10-27 2013-05-02 Merck Sharp & Dohme Corp. Novel compounds that are erk inhibitors
PH12014500814A1 (en) * 2011-11-04 2014-05-19 Hoffmann La Roche New aryl-quinoline derivatives
US20150299696A1 (en) 2012-05-02 2015-10-22 Sirna Therapeutics, Inc. SHORT INTERFERING NUCLEIC ACID (siNA) COMPOSITIONS
UA110688C2 (en) 2012-09-21 2016-01-25 Пфайзер Інк. Bicyclic pirydynony
BR112015006990A2 (en) 2012-09-28 2017-07-04 Merck Sharp & Dohme compound, pharmaceutical composition, and use of at least one compound
PL2925888T3 (en) 2012-11-28 2018-03-30 Merck Sharp & Dohme Corp. Compositions and methods for treating cancer
WO2014100065A1 (en) 2012-12-20 2014-06-26 Merck Sharp & Dohme Corp. Substituted imidazopyridines as hdm2 inhibitors
US9540377B2 (en) 2013-01-30 2017-01-10 Merck Sharp & Dohme Corp. 2,6,7,8 substituted purines as HDM2 inhibitors
US20160194368A1 (en) 2013-09-03 2016-07-07 Moderna Therapeutics, Inc. Circular polynucleotides
AR098776A1 (en) * 2013-12-18 2016-06-15 Chiesi Farm Spa ISOCROMENE DERIVATIVES AS INHIBITORS OF PHOSFOINOSITIDO-3 KINASES
CN107406445B (en) 2015-02-03 2019-12-24 辉瑞公司 Novel cyclopropylbenzofurylpyridopyrazine diketones
TWI773657B (en) 2015-12-18 2022-08-11 美商亞德利克斯公司 Substituted 4-phenyl pyridine compounds as non-systemic tgr5 agonists
US12084472B2 (en) 2015-12-18 2024-09-10 Ardelyx, Inc. Substituted 4-phenyl pyridine compounds as non-systemic TGR5 agonists
WO2018071283A1 (en) 2016-10-12 2018-04-19 Merck Sharp & Dohme Corp. Kdm5 inhibitors
CN106946897B (en) * 2017-02-28 2018-10-23 牡丹江医学院 A kind of drug that treating cholecystitis and its application
EP3706742B1 (en) 2017-11-08 2023-03-15 Merck Sharp & Dohme LLC Prmt5 inhibitors
WO2019094312A1 (en) 2017-11-08 2019-05-16 Merck Sharp & Dohme Corp. Prmt5 inhibitors
MX2021001486A (en) 2018-08-07 2021-07-15 Merck Sharp & Dohme Llc Prmt5 inhibitors.
EP3833668B1 (en) 2018-08-07 2025-03-19 Merck Sharp & Dohme LLC Prmt5 inhibitors
US11981701B2 (en) 2018-08-07 2024-05-14 Merck Sharp & Dohme Llc PRMT5 inhibitors
US11731970B1 (en) 2023-03-23 2023-08-22 King Faisal University Pyrrolo[2,3-b]quinoline compounds as antibacterial agents
WO2024206339A1 (en) 2023-03-27 2024-10-03 Edgewise Therapeutics, Inc. Quinolinone amide compounds and uses thereof
WO2025207665A1 (en) * 2024-03-26 2025-10-02 Edgewise Therapeutics, Inc. Quinolinone compounds and uses thereof

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3509156A (en) * 1967-12-08 1970-04-28 American Home Prod 1,2-dihydro-2-oxo-3-quinolineacetamides and related intermediates
NO133758C (en) * 1970-04-04 1976-06-23 Takeda Chemical Industries Ltd
AU577105B2 (en) * 1985-04-02 1988-09-15 T.P.O. :Pharmachim: Acylaminic penicillin derivatives
IE892088L (en) * 1988-07-12 1990-01-12 William Henry Deryk Morris Quinoline derivatives, their production and use
TW205037B (en) * 1989-10-06 1993-05-01 Takeda Pharm Industry Co Ltd
JPH03181465A (en) * 1989-12-11 1991-08-07 Takeda Chem Ind Ltd Quinoline derivative
ATE116645T1 (en) * 1990-02-10 1995-01-15 Takeda Chemical Industries Ltd CHROME DERIVATIVES, THEIR PRODUCTION AND USE.
JPH059179A (en) * 1990-09-27 1993-01-19 Takeda Chem Ind Ltd Heterocyclic compound, its production and acat inhibitor
DE69110828T2 (en) * 1990-10-16 1995-11-30 Takeda Chemical Industries Ltd Heterocyclic amine derivatives, their preparation and their use.
IL99731A0 (en) * 1990-10-18 1992-08-18 Merck & Co Inc Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them
EP0634402A1 (en) * 1993-07-14 1995-01-18 Takeda Chemical Industries, Ltd. Isochinolinone derivatives, their production and use

Also Published As

Publication number Publication date
HUT67284A (en) 1995-03-28
CA2105518C (en) 2005-08-09
NO933133D0 (en) 1993-09-02
CN1090274A (en) 1994-08-03
ATE161530T1 (en) 1998-01-15
EP0585913A2 (en) 1994-03-09
HU9302499D0 (en) 1993-11-29
EP0585913A3 (en) 1994-05-25
US5700810A (en) 1997-12-23
FI933857A7 (en) 1994-05-17
IL106908A0 (en) 1993-12-28
NZ248583A (en) 1995-04-27
AU4613293A (en) 1994-03-10
NO933133L (en) 1994-03-07
AU667739B2 (en) 1996-04-04
CA2105518A1 (en) 1994-03-05
DE69315920D1 (en) 1998-02-05
KR940007003A (en) 1994-04-26
NO179904B (en) 1996-09-30
DE69315920T2 (en) 1998-06-10
US5482967A (en) 1996-01-09
FI933857A0 (en) 1993-09-03
EP0585913B1 (en) 1997-12-29

Similar Documents

Publication Publication Date Title
NO179904C (en) Condensed heterocyclic compounds and their use
DE69321525D1 (en) MORPHINAN DERIVATIVES AND MEDICAL USE
ATE241625T1 (en) HETEROCYCLIC COMPOUNDS, THEIR PRODUCTION AND USE
DK0562439T3 (en) Triazolopyridazine Compounds, Their Preparation and Use
ATE369337T1 (en) NEW BIZYCLIC COMPOUNDS
NO942372L (en) -propenoic acid derivative
DE68905407D1 (en) ANALGETIC CARBONIC ACID DERIVATIVES.
DE69216873D1 (en) Benzene derivatives to promote the production of the nerve growth factor
ATE238298T1 (en) TETRADERIVATIVES, THEIR PRODUCTION AND USE
AU755654C (en) Novel amide compounds and drugs containing the same
FI941863A0 (en) oxazolidone derivative
DE69004598D1 (en) 6-Amino-6-deoxyfumagillole, their preparation and their use.
ATE137747T1 (en) AMINOBENZENE COMPOUNDS, PRODUCTION AND USE
ATE81651T1 (en) SUBSTITUTED AROMATIC COMPOUNDS WITH CENTRAL NERVOUS SYSTEM ACTION.
DE69607890D1 (en) Aromatic hydroxamic acid compounds, their production and use
ATE80162T1 (en) ANTIBIOTIC ISOXAZOLE DERIVATIVES, THEIR PRODUCTION AND USE.
ATE92480T1 (en) OXADIAZOLE COMPOUNDS, THEIR PRODUCTION AND USE AS PESTICIDES.
ATE143591T1 (en) USE OF BIS-(P-HYDROXYPHENYLTHIO)METHANE DERIVATIVES TO INHIBIT THE PROGRESSIVE DEVELOPMENT OF INSULIN-DEPENDENT DIABETES MELLITUS
DE68910736D1 (en) Fungicidal heterocyclic nitrogen compounds.
ATE264844T1 (en) TETRAHYDROISOCHINOLINALKANOL DERIVATIVES AND PHARMACEUTICAL PREPARATIONS CONTAINING SAME